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Case Reports in Dermatology, ISSN 1662-6567, 08/2017, Volume 9, Issue 2, pp. 112 - 118
Aplasia cutis congenita type VI, also known as Bart syndrome, is a rare genetic mechanobullous disorder characterized by congenital localized absence of skin,... 
Bart syndrome | Aplasia cutis congenita type VI | Epidermolysis bullosa | Conservative treatment | Wound healing | Congenital diseases | Family medical history | Childbirth & labor
Journal Article
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